Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Ahlam F. Al-Salhoob"'
Autor:
Abdullah M.A. Al Majid, Mohammad Shahidul Islam, Zeid Abdullah Al-Othman, Ahlam F. Al-Salhoob
Publikováno v:
Arabian Journal of Chemistry, Vol 10, Iss S1, Pp S964-S970 (2017)
A set of chiral bis-amide ligands (4a–d and 5a–d) were obtained easily from readily available starting materials in a straightforward manner via acid chloride reaction of the parent Feist’s acid. These ligands have been tested as chiral catalys
Externí odkaz:
https://doaj.org/article/ff760861fc83499cb9a9f722659ae1da
Autor:
Assem Barakat, Zeid Abdullah Al-Othman, Ahlam F. Al-Salhoob, Abdullah M. A. Al Majid, Mohammad Shahidul Islam
Publikováno v:
Molecules, Vol 17, Iss 5, Pp 5550-5563 (2012)
The hemilabile chiral C2 symmetrical bidentate substituted amide ligands (1R,2R)-5a-d and (1S,2S)-6a-d were synthesized in quantitative yield from (1R,2R)-(+)-3-methylenecyclo-propane-1,2-dicarboxylic acid (1R,2R)-3 and (1S,2S)-(-)-3-methylene-cyclop
Externí odkaz:
https://doaj.org/article/9f2adfef9ee2490eb90a05c0ac748cf8
Autor:
Zeid A. ALOthman, Mohammad Shahidul Islam, Assem Barakat, Ahlam F. Al-Salhoob, Abdullah M.A. Al Majid
Publikováno v:
Molecules. 17:5550-5563
The hemilabile chiral C 2 symmetrical bidentate substituted amide ligands (1 R ,2 R )- 5 a-d and (1 S ,2 S )- 6 a-d were synthesized in quantitative yield from (1 R ,2 R )-(+)-3-methylenecyclo-propane-1,2-dicarboxylic acid (1 R ,2 R )- 3 and (1 S ,2
Publikováno v:
Arabian Journal of Chemistry, Vol 10, Iss S1, Pp S964-S970 (2017)
A set of chiral bis-amide ligands (4a–d and 5a–d) were obtained easily from readily available starting materials in a straightforward manner via acid chloride reaction of the parent Feist’s acid. These ligands have been tested as chiral catalys
Autor:
Abdullah M A, Al Majid, Mohammad Shahidul, Islam, Zeid Abdullah, Al-Othman, Ahlam F, Al-Salhoob, Assem, Barakat
Publikováno v:
Molecules
The hemilabile chiral C2 symmetrical bidentate substituted amide ligands (1R,2R)-5(a-d) and (1S,2S)-6(a-d) were synthesized in quantitative yield from (1R,2R)-(+)-3-methylenecyclo-propane-1,2-dicarboxylic acid (1R,2R)-3 and (1S,2S)-(-)-3-methylene-cy